Variant #0000808859 (NC_000019.9:g.39412664G>A, NC_000019.9(NM_017827.3):c.393+214C>T (SARS2))

Chromosome 19
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.39412664G>A
DNA change (hg38) -
Published as SARS2(NM_001145901.1):c.448C>T (p.P150S)
ISCN -
DB-ID SARS2_000012
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00039 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SARS2 NM_001145901.1 -?/. - c.448C>T r.(?) p.(Pro150Ser)
SARS2 NM_017827.3 -?/. - c.393+214C>T r.(=) p.(=)


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